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Produces Home Study reports and provides recommendations within the specified timeframe. Master's degree in social work, psychology, sociology, or other relevant behavioral science in which direct clinical experience is a program requirement.
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This position will focus on leveraging mouse models, human pluripotent stem cells, and engineered vascular models combined with single cell technologies and computational approaches to study the dynamics of normal developmental hematopoiesis and the prenatal origins of pediatric leukemias.
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Strong experience in patient centered outcomes research: COA instrument development/psychometric validation, quantitative analysis of CObased clinical study endpoints, regulatory dossier development and submissions.
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Candidates are required to possess an advanced degree in occupational therapy or behavioral sciences and must be eligible for licensure to practice in the state of WA as one of the following: Psychologist, Mental Health Counselor, Occupational Therapist, Marriage and Family Therapist Counselor, Advanced Social Worker, or Independent Clinical Social Worker.
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Based at Fred Hutch and reporting to the Project Manager, the Clinical Research Coordinator will serve as an integral member of the pediatric research program to manage bone marrow transplant, gene therapy and other pediatric clinical trials from start-up to close-out.
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Our global Clinical Operations colleagues within our PPD clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts.
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The Clinical Research Assistant will work closely with the Center for Interventional Immunology study team to recruit and enroll participants, with and without autoimmune disease, conduct study visits and maintain study records in accordance with specified protocol and procedures for the Translational Research Program Immune Mediated Disease Registry and Repository.
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Clinical Research Budget Analyst II reviews the Medicare coverage analysis based on available study documents, such as protocol, proposed budget, and informed consent, and captures all clinical costs and investigators and study team efforts required to carry out the study, as well as costs for ancillary services.
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Understand research study flow, work with clinic staff, support services and research team as needed to implement clinical trials. Work with Regulatory Coordinator to ensure that reporting to the Institutional Review Board (IRB) and study sponsors are timely, accurate and satisfy applicable regulation.
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Six or more years of experience in medical records, cancer registry, clinical study coordination or related field. This individual will work under limited supervision of the Clinical Research Operations Manager and will be required to perform their responsibilities with a high level of independence within the scope of study protocol(s) and institutional policies and guidelines.
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Understands clinical trial operational complexities from study start up through enrollment, quality assurance, and study readout. A minimum of 10 years in the drug development & commercialization process, Health Authorities and/or academic experience, and clinical trial design with proven progression in relevant roles.
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The Clinical Affairs Scientific Study Manager for Beckman Coulter Diagnostics is responsible for Managing the In-Vitro Diagnostic Clinical Research for the Neurodegenerative Disease Portfolio.
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The RoleThe Associate Director/Director, Clinical Science provides leadership in the areas of development and execution of analytical plans for CIVO clinical study protocols, external clinical partner relationship management, and working with cross-functional teams to shape the companys alliances and CIVO clinical program strategy.
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Main responsibilities include, but are not limited to, the review of New Study routing forms and essential study start-up documents, the itemized cost analysis and interpretation of clinical protocols into budgets milestones, provide accurate patient cost descriptions for the ICF to be submitted to the IRB, and update budget, milestones, and ICF information as necessary per contract/protocol amendments.
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Must be at least 21 years of age High school diploma or high school equivalency course of study (GED/HSEC) with 2 years of directly relevant experience (professional or volunteer) working with children and youth in one of the following settings: daycare or family home setting as a nanny, day camp, school, sports, or child placing agency.
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